• Clinical Trial Assitant 3 Jobs in United States Of America - 25368586

  • Iqvia
  • United States Of America, Usa
  • Save Job
  • 5 - 8 Years
  • Posted : above 1 month

Job Description:

IQVIA is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward

PURPOSE

Provide administrative support to clinical projects and update clinical systems and databases Assists with general administrative functions, as required, in support of designated clinical team members

RESPONSIBILITIES

Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines
Collaborate with Clinical Project Manager (CPM), CRAs/iCRAs and RSU on the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures Assist with periodic review of study files and completeness
Collaborate with CRAs/iCRAs and RSU on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information
Coordinate the tracking and management of Case Report Forms (CRFs), queries and clinical data flow
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
Assist in training and orienting new staff May act as a mentor for less experienced CTAs
May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training and with required approval
Perform assigned administrative tasks to support team members with clinical trial execution

REQUIRED KNOWLEDGE, SKILLS AND ABILITIES

Basic knowledge of applicable clinical research regulatory requirements; ie, Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Knowledge of applicable protocol requirements as provided in company training
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
Effective written and verbal communication skills including good command of English language
Effective time management and organizational skills
Ability to establish and maintain effective working relationships with coworkers, managers and clients

MINIMUM REQUIRED EDUCATION AND EXPERIENCE

High or Secondary School diploma/certificate or countrys educational equivalent and 5 years applicable experience; or equivalent combination of education, training and experience

Join Us

Making a positive impact on human health takes insight, curiosity, and intellectual courage It takes brave minds, pushing the boundaries to transform healthcare Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients

Forge a career with greater purpose, make an impact, and never stop learning

Job ID R1108064

Profile Summary:

Employment Type : Full Time
Eligibility : Any Graduate
Industry : Consulting Services
Functional Area : Bio Tech/R&D/Scientist
Role : Clinical Research
Salary : As per Industry Standards
Deadline : 09th Jun 2020

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